I already wrote about the research of my friend Olga Amosova  who studied the sickle-cell anemia mutation. She and her colleagues  needed to store short fragments of hemoglobin genes for their  experiments. All the fragments were identical. They noticed that with  time the fragments always broke down in the same place. It was a  mystery. When good scientists stumble on a mystery, they start digging.
They found that one of the nucleotides rips off the DNA fragment at the  site of the Sickle-cell mutation. That place on the DNA becomes fragile  and later breaks down. These sites need to be repaired. The repair is  very error-prone and often leads to a mutation.
When DNA strands are left unattended, they want to pair up. There are  four types of nucleotides: A, C, G and T. So mathematically the fragment  of DNA is a string in the alphabet A, C, G, T. These nucleotides are  matched to each other. When two DNA strands pair up, A on one strand  always matches T and C matches G. So it is logical that if there are two  complementary DNA pieces on the same fragment, they will find each  other and pair up. They form a hydrogen bond. For example, a piece AACGT  matches perfectly another piece TTGCA. Suppose a substring of DNA  consists of a piece AACGT and somewhere later the reverse of the match:  ACGTT. Such a string is called an inverted repeat. The DNA fragment I  mentioned contains a string AACGT****ACGTT. Two pieces AACGT and ACGTT  are complementary and not too far from each other in space. So it is  easy for them to find each other and to bond to form a so-called  stem-loop or a hairpin structure. The site of Sickle-cell mutation falls  into the loop.
Olga and her colleagues discovered that for some particular loops the  orientation in space becomes awkward and one of the nucleotides rips  off. Such a rip off is called depurination. In further investigation,  Olga found examples of when depurination happens. The first sequence of  the pair that will bond later has to have at least five nucleotides and  has to end in T. Correspondingly the second part in the pair has to  begin with A. In the middle there needs to be four nucleotides GTGG. The  first G flies away. Enzymes rush like a first aid squad to repair it  and introduce mistakes that lead to mutation and diseases like cancer.
DNA was thought to be simply a passive information storage system, not  capable of any action. Now we see that DNA is capable of action. DNA can  damage itself. Damage provokes a mutation. For all practical purposes  it is self-mutilation. Olga and her colleagues scanned the human genome  for other sequences that are capable of self-mutilation. They found that  such sequences are overwhelmingly present. They are present in much  higher numbers than would be expected statistically. The pieces that are  capable of damaging themselves occur 40 times more often than would  occur if the nucleotides were distributed randomly. They are especially  overrepresented in genes linked to cancer.
Self-damaging shouldn’t happen in normal situations. It can be provoked  by the environment, for example, the chemistry of the cell. That means,  that our cancers are not only in our genes but also in our life-style.  There was, for example, a suggestion in a recent NY Times article, Is Sugar Toxic?,  that too much sugar in a diet might provoke cancer. If the rate of  mutation depends on the environment, we can influence it and prolong our  lives.
It is not clear why the ability to self-mutilate survives in the  evolutionary process. It is quite possible that if something very bad  happens to our planet, we need our genes to be able to mutate very fast  in order to adjust to the environment so that humans can survive.
Though I never tried to donate my sperm to a sperm bank, because of my  inability to produce it, I know that sperm banks look for people who  have ancestors who lived for a very long time. Such sperm is in bigger  demand as everyone wants their children to live longer. I wonder if this  tendency is a mistake. Global warming is upon us. People with longevity  genes might not be flexible enough for their children to survive the  changing of the Earth.
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